K-number	K193139
Device name	ProVecta 3D Prime Ceph
Applicant	Durr Dental SE
Product code	OAS
Device class	Class II
Decision date	Mar 5, 2020
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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ProVecta 3D Prime Ceph

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